Abstract: In a process for purifying crude anthraquinone obtained by the oxidation, by molecular oxygen in an aqueous alkali metal hydroxide solution, of an adduct obtained by the Diels-Alder reaction of butadiene with 1,4-naphthoquinone obtained by a catalytic vapor phase oxidation reaction of naphthalene, an improvement characterized in that said crude anthraquinone is subjected to oxidation treatment in an aqueous medium in the presence of a hypochlorite.
Abstract: A heat-sensitive recording sheet having a color-forming layer comprising a colorless or pale-colored chromogenic dyestuff and a hydroxyphthalic acid diester having a melting point of from about 60.degree. to about 120.degree. C.
Abstract: 1,4,4a,9a-Tetrahydroanthraquinone compounds are produced by Diels-Alder reaction of 1,4-naphthoquinone with a conjugated diolefin in the 1,4,4a,9a-tetrahydroanthraquinone compound as a reaction medium.
Abstract: A hydroanthraquinone is produced from a reaction mixture obtained by the Diels-Alder reaction of naphthoquinone with a conjugated diolefin in an inert organic solvent. The reaction mixture in an inert organic solvent is oxidized with an oxidizing agent to decompose quinhydrone or quinhydrone derivative produced by said Diels-Alder reaction and the crystallized hydroanthraquinones are separated from said inert organic solvent.
Abstract: A highly chlorinated copper phthalocyanine is produced by chlorinating a copper phthalocyanine in the presence of a catalyst for chlorination in a solvent by charging chlorine under an elevated pressure. The chlorination is carried out in an inert organic solvent incorporating chlorosulfonic acid and/or pyrosulfuryl chloride at a ratio of 1 to 30 wt. % based on said inert organic solvent which maintain dispersibility of said resulting highly chlorinated copper phthalocyanine.
Abstract: A scale deposition from an aqueous slurry of naphthoquinone and phthalic acid can be prevented by adding fine crystals of phthalic acid to the aqueous slurry of naphthoquinone and phthalic acid collected, which slurry is obtained by contacting a gas resulting from a catalytic gas phase oxidation of naphthalene with water or a mother liquor recycled. The fine crystals of phthalic acid have diameters of less than 100.mu., preferably 10 to 40.mu., and can be in an aqueous slurry of phthalic acid pulverized by a pulverizer.
Abstract: A crude naphthoquinone produced by an oxidation of naphthalene is purified by a reduced pressure distillation of a crude 1,4-naphthoquinone having an acid content of less than 5 equivalent % calculated as monobasic acid and the crude naphthoquinone is preferably treated by an oxidation of oxidizable impurities.
Abstract: 1,4-Dihydroanthraquinones are produced by oxidizing 1,4,4a,9a-tetrahydroanthraquinone or 1,4-dihydroanthrahydroquinone or an inert substituted derivative thereof with molecular oxygen in an aqueous medium at the reaction temperature of lower than 70.degree. C. under the condition of pH of 8.5 to 12.
Abstract: Benzanthrone is produced by reacting a hydroanthraquinone having 1,4-dihydro ring with acrolein or an acrolein precursor in the presence of a dehydration catalyst.
Abstract: Anthrone is produced by an intramolecular condensation of hydroanthraquinone such as tetrahydroanthraquinone or dihydroanthrahydroquinone by heating it in the absence of oxygen with or without an inert solvent.